# Randox Laboratories, Limited – FDA Inspection, Apr 28, 2016

Source: https://www.keypedia.com/records/fda_inspections/randox-laboratories-limited/441a0146-d9ca-43ce-a728-7b45707e020d
Source feed: FDA_Inspections

> FDA inspection 969545 of Randox Laboratories, Limited, April 28, 2016. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 969545
- Company Name: Randox Laboratories, Limited
- Inspection Date: 2016-04-28
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 1015099 - 2017-06-01
- [FDA Inspection 969514 - 2016-04-28](https://www.keypedia.com/records/fda_inspections/randox-laboratories-limited/b853afcb-4867-4185-a251-15dda3910551)
- [FDA Inspection 817316 - 2012-11-29](https://www.keypedia.com/records/fda_inspections/randox-laboratories-limited/ba313df0-02c5-48c9-a6f4-682bb787683b)

Company: https://www.keypedia.com/companies/randox-laboratories-limited/8a08dce9-5103-4fad-a76a-546f1df5aa53

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7